Fluid flow control by a non-pinching valve
A pumping system comprising a pump comprising a door for access within a housing of the pump, a pump segment configured for conveying a fluid based on compression of the pump segment, a pump segment frame for preventing said pump segment from stretching, a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in the housing, and a non-pinching valve configured to be disposed in the housing and to control a flow of the fluid without requiring pinching of a tube.
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Controlling the fluid flow of a medical pump system, such as an infusion pump, by a clamping an intravenous (IV) tube can deleterious affect operation of the medical pump system. Clamping mechanisms, such as a roller clamp, screw clamp, slide clamp, compress a tube to control the fluid flow. For example, the slide clamp has a graduated opening through which the tube passes. Pushing the tube into the narrow end of the opening compresses the tube and reduces the flow rate of the fluid flow through the tube. In contrast, sliding towards the wide end of the opening decreases the compression of the tube and thus, increases the flow rate through the tube. Also, the tube may be shipped and/or stored for long periods of time with the clamping mechanism continually applying pressure to the tube.
As a result of the compression of the tube, the tube may be damaged and/or deformed. For example, the tube is permanently deformed and thus, restricts fluid flow.
Moreover, clinicians may improperly insert/remove components from the pump housing. For example, it may be difficult for the clinician to visually determine where certain components (e.g., clamping device, pumping segment, etc.) are to be placed within the pump housing. As a result, the clinician may place the components in the wrong position which negatively affects the pumping operation.
SUMMARYIn one or more embodiments, a valve is provided. The valve includes a first port and a second port. The valve also includes a slidable cover configured for controlling flow of a fluid through the first and second ports. The slidable cover is slidably disposed over the first and second ports. The slidable cover includes a fluid flow channel configured to allow the fluid to flow through the first and second ports when the channel is disposed over the first port and second ports.
In one or more embodiments, a non-pinching valve system is provided. The non-pinching valve system includes a pump configured for pumping a fluid in a medical environment and a tube configured for conveyance of the fluid. The non-pinching valve system also includes a non-pinching valve configured to be disposed in a pump housing and to control a flow of the fluid without requiring pinching of the tube. The tube is releasably attached to the non-pinching valve. The non-pinching valve includes first and second ports, wherein the first and second ports are not required to be coaxial.
In one or more embodiments, a non-pinching valve system is provided. The non-pinching valve system includes a pump configured for pumping a fluid in a medical environment and a tube configured for conveyance of the fluid. The non-pinching valve system also includes a non-pinching valve configured to be disposed in a pump housing and to control a flow of the fluid without requiring pinching of the tube, wherein the tube is releasably attached to the non-pinching valve. The non-pinching valve includes a housing having first and second ports, and a slidable cover configured for controlling flow of the fluid through the first and second ports. The slidable cover is slidably disposed over the first and second ports. The slidable cover includes a fluid flow channel configured to allow the fluid to flow through the first and second ports when the channel is disposed over the first and second ports.
In one or more embodiments, a pump segment frame system is provided. The pump segment frame system includes a pump segment frame having first and second distal ends, wherein a pump segment is attached to the first and second distal ends for preventing the pump segment from stretching. The pump segment frame system also includes a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in a housing of a pump.
In one or more embodiments, a pumping system is provided. The pumping system includes a pump configured for pumping a fluid in a medical environment, the pump including a door for access within a housing of the pump. The pumping system also includes a pump segment configured for conveying the fluid based on compression of the pump segment generated by the pump, and a pump segment frame. The pump segment frame includes first and second distal ends, wherein the pump segment is attached to the first and second distal ends for preventing the pump segment from stretching. The pump segment frame also includes a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in the housing. The pumping system further includes a non-pinching valve configured to be disposed in the housing and to control a flow of the fluid without requiring pinching of a tube.
In one or more embodiments, a method of controlling a fluid flow is provided. The method includes actuating a non-pinching valve to a closed position by rotating a slidable cover axially over a housing of the non-pinching valve, wherein the non-pinching valve controls flow of a fluid without requiring pinching of a tube attached to the non-pinching valve. The method also includes placing the non-pinching valve in a housing of an infusion pump and closing a door of the infusion pump to close access in the housing. The method further includes in response to the closing of the door, actuating the non-pinching valve to an open position, by the door, such that fluid flows through the non-pinching valve.
Additional features and advantages of the disclosure will be set forth in the description below and, in part, will be apparent from the description or may be learned by practice of the disclosure. The objectives and other advantages of the disclosure will be realized and attained by the structure particularly pointed out in the written description and claims hereof as well as the appended drawings.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the disclosure as claimed.
The drawings referred to in this description should be understood as not being drawn to scale except if specifically noted.
DESCRIPTION OF EMBODIMENTSReference will now be made in detail to embodiments of the present technology, examples of which are illustrated in the accompanying drawings. While the technology will be described in conjunction with various embodiment(s), it will be understood that they are not intended to limit the present technology to these embodiments. On the contrary, the present technology is intended to cover alternatives, modifications and equivalents, which may be included within the spirit and scope of the various embodiments as defined by the appended claims.
Furthermore, in the following description of embodiments, numerous specific details are set forth in order to provide a thorough understanding of the present technology. However, the present technology may be practiced without these specific details. In other instances, well known methods, procedures, components, and circuits have not been described in detail as not to unnecessarily obscure aspects of the present embodiments.
Pump 110 includes housing 115, door 119 and user interface 117. In one embodiment, pump 110 is an infusion pump. For example, fluid from an intravenous (IV) bag (not shown) is pumped to a patient (not shown) as indicted by fluid flow 125.
User interface 117 can include a display, buttons, controls, etc. for use by a clinician to facilitate in control of pumping system 100.
Housing 115 is configured to hold the components of pump 110, as will be described in detail below.
Door 119 is removable or hinged with respect to housing 115. For example, door 119 is the entire front face of pump 110 and is removable from housing 115 to provide access within housing 115. It should be understood that door 119 (or lid) can be any dimension, shape, orientation that enables access for proper placement and/or removal of components from within housing 115.
Pump 110 also includes pumping segment 130, pumping fingers 131, non-pinching valve 140, and coupler 150.
Pumping segment 130 is configured to be easily compressed by fingers 131. For example, pumping segment 130 is a silicone rubber tube.
In one embodiment, tubes 120 and 121 are comprised of the same material and pumping segment is comprised of a more pliable material, such as silicone. It should be understood that pumping segment 130 can be any material that is conducive to being compressed by fingers 131.
Pumping segment 130 is fluidly connected to tube 120 via non-pinching valve 140 and fluidly connected to tube 121 via coupler 150. For example, in one embodiment, outer diameter of tube 121 mates with the inner diameter of interface 152. Similarly, the outer diameter of segment 130 mates with the inner diameter of interface 151. In another embodiment, the inner diameter of pumping segment 130 mates with the outer diameter of interface 144. Similarly, the inner diameter of tube 120 mates with the outer diameter of interface 143. It should be understood that pumping segment 130 can be fluidly connected to tubes 120 and 121 by any coupling means.
In one embodiment, coupler 150 is a “Y” coupler that accommodates two different tubes (e.g., tube 121 and another tube (not shown)). For example, tube 121 conveys a first type of fluid (e.g., a first type of medicine) and the other tube conveys a second type of fluid (e.g., a second type of medicine). Accordingly, the different types of fluid may mix at coupler 150 and the mixture of fluid is pumped by pumping system 100.
Pumping fingers 131 are configured to compress pumping segment 130 to pump fluid. For example, fingers 131 press on pumping segment 130 in sequence. In particular, fingers 131 compress pumping segment 130 against a platen (not shown). As a result, fluid flow 125 is generated.
Non-pinching valve 140 is configured to control fluid flow 125 in pumping system 100 without requiring pinching of a tube (e.g. 120). In other words, non-pinching valve 140 controls fluid flow 125 without applying pressure to an outer surface of a tube and thereby not compressing the tube. In one embodiment, non-pinching valve 140 is a stop cock. Non-pinching valve 140 can be any valving system that controls fluid flow 125 without compressing a tube. It should be appreciated that non-pinching valve 140 and a connected tube (e.g., tube 120) can be shipped and/or stored in the closed or open position without damaging the tube.
In general, when channel 250 is aligned with ports 241 and 242, fluid flow 125 flows through channel 250 and subsequently through non-pinching valve 240A. In contrast, when channel 250 is not aligned with ports 241 and 242, fluid flow 125 does not flow through channel 250 and thus, not through non-pinching valve 240A
In one embodiment, housing 210 and shaft 220 are cylindrical. For example, fluid flow 125 is stopped when channel 250 is not aligned with ports 241 and 242. In such an example, a clinician rotates handle 230 (e.g., 90 degrees from the depicted position) such that channel 250 is not aligned with ports 241 and 242. Accordingly, shaft 220 seals ports 242 and 241 such that fluid flow is stopped and does not flow through channel 250.
It should be understood that channel 250 rotates perpendicularly to the direction of fluid flow 125. Moreover, interfaces 143 and 144 and channel 250 are coaxial or collinear with one another. Accordingly, fluid flow 125 can occur in two discrete positions of shaft 220. The first position, is as depicted. The second position is shaft 220 rotated 180 degrees (from the depicted position).
In one embodiment, the cross-sectional shape (e.g. circular) and diameter of ports 241 and 242, and channel 250 are the same. In another embodiment, the cross-sectional shape of channel 280 is different (e.g., oval, tear drop, etc.) than the cross-sectional shape of ports 241 and 242 to facilitate in manual regulation of fluid flow 125.
In various embodiments, housing 210 and shaft 220 are comprised of a rigid or semi-rigid material.
Accordingly, in one embodiment, channel 250 is aligned with ports 241 and 242 at one position. For example, if shaft 220 is rotated to any other position (other than the depicted position), then fluid does not flow through channel 250.
Accordingly, in one embodiment, channel 250 is aligned with ports 241 and 242 at a single position. For example, if shaft 220 is rotated to any other position (other than the depicted position), then fluid does not flow through channel 250.
Slidable cover 330 is configured to slide with respect to housing 310 to control fluid flow 125. Slidable cover 330 includes channel 335.
In particular, fluid flow 125 occurs between housing 310 and slidable cover 330 via channel 335. As such, fluid flow 125 flows along the outer surface or periphery of housing 310.
In one embodiment, housing 310 and slidable cover 330 are cylindrical.
In another embodiment, channels 360 and 361 are disposed along the center axis of housing 310. Accordingly, slidable cover 330 slides axially with respect to housing 310 and channels 360 and 361. Also, slidable cover 330 slides axially with respect to portions of fluid flow 125.
Referring now to
Interfaces 443 and 444 are configured to couple tubes to non-pinching valve 440A.
Handle 450 facilitates in rotating slidable cover 430 along an axis of non-pinching valve 440A.
Handle 452 facilitates a clinician in placing or seating non-pinching valve 440A into housing 115. For example, a clinician grasps handle 452 while placing non-pinching valve 440A into housing 115 or removing non-pinching valve 440A from housing 115.
Visual indicator 480 is configured to facilitate a clinician in properly placing non-pinching valve 440A in housing 115, which will be described in detail below.
Locking mechanism 460A is a tab that is seated in slot 461A such that non-pinching valve 440A is locked in either an open or closed position (or any other designated position, such as one half flow rate). In order to unlock non-pinching valve 440A, locking mechanism 460A is pushed out of slot 461 such that it is able to travel along slot 462A.
Referring now to
Non-pinching valve 440B also includes graduation markings 470. Each graduation marking is indicative of a particular flow rate. Accordingly, graduation markings facilitate in controlling the flow rate through non-pinching valve 440B. In a further embodiment, graduation markings 470 are coupled with a tactile and/or audible indication. For example, when the non-pinching valve is actuated according to the graduation markings, the clinician may feel a tactile response and/or an audible response, such as a click.
Referring now to
In various embodiments, a non-pinching valve (e.g., non-pinching valve 240A) is actuated to an open position in response to the closing of door 119. In particular, door 119 comprises an engagement feature (not shown) that mechanically engages with a handle (e.g., handle 230). For example, the engagement feature has particular beveled features that engage with the handle and actuate the handle, such that the non-pinching valve is actuated from the closed position to the open position, when door 119 is pressed into place.
In another embodiment, a non-pinching valve (e.g., non-pinching valve 240A) is actuated to a closed position in response to the opening of door 119. In particular, door 119 comprises an engagement feature (not shown) that mechanically engages with a handle (e.g., handle 230). For example, the engagement feature mechanically engages with the handle, such that the non-pinching valve is actuated from the open position to the closed position, when door 119 is opened or removed from housing 115.
It should be appreciated that a non-pinching valve can be utilized without the use of a pump. For example, in a gravity fed fluid flow system, the non-pinching valve can be utilized to control flow of fluid to a patient.
Frame 510 is configured to prevent pumping segment 130 from stretching.
In particular, distal ends of pumping segment 130 are attached to corresponding distal ends of frame 510, which is comprised of a rigid or semi-rigid material. Accordingly, pumping segment 130 is prevented from stretching.
In contrast, in a conventional system, if a pumping segment is stretched, for example when a clinician places the pumping segment in the housing, then the pumping segment is likely to be improperly placed in the housing. As a result, the operation of the pumping system is negatively affected.
In one embodiment, non-pinching valve 140 is disposed at a distal end of frame 510. As such, a distal end of pumping segment 130 is attached to non-pinching valve 140.
In another embodiment, coupler 150 is attached to a distal end of frame 510. As such, a distal end of pumping segment 130 is attached to coupler 150.
System 500 also includes visual indicators 580 and 581. In general, visual indicators 580 and 581 facilitate in the proper placement of system 500 into housing 115. For example, housing 115 includes visual indicators corresponding to visual indicators 580 and 581. The corresponding visual indicators in housing 115 can be an outline, indention, etc. that corresponds to visual indicators 580 and 581. As a result, system 500 is properly placed in housing 115 such that pumping system 100 operates correctly.
In various embodiments, the corresponding visual indicators in housing 115 can be a color or an outline of components (e.g., outline of non-pinching valve 140, frame 510, coupler 150, etc.).
Frame 610 is configured to prevent pumping segment 130 from stretching, as described above. For example, distal ends of pumping segment 130 are attached to corresponding distal ends of frame 610, which is comprised of a rigid or semi-rigid material. Accordingly, pumping segment 130 is prevented from stretching.
Frame 610 is further configured to be a platen. For example, fingers 131 extend within housing 115 and compress pumping segment 130 against frame 610. Moreover, the placement of pumping segment 130 with respect to frame 610 provides a consistent gap (e.g., between pumping segment 130 and frame 610) to facilitate in pumping and pressure sensing.
In one embodiment, frame 610 includes a window such that pumping segment 130 is viewable during use of pumping system 100.
In one embodiment, a non-pinching valve (e.g., non-pinching valve 240A) is disposed at a distal end of frame 610. As such, a distal end of pumping segment 130 is attached to the non-pinching valve. In such an embodiment, frame 610 is interposed between housing 210 and handle 230.
In another embodiment, coupler 650 is attached to a distal end of frame 610. As such, a distal end of pumping segment 130 is attached to coupler 671.
System 600 also includes retainers 670 and 671 that facilitate in retaining pumping segment 130 on housing 210 and coupler 650. In particular, retainers 670 and 671 clamp the distal ends of pumping segment 130 on interface 144 and coupler 650.
It should be understood that pumping segment 130 may be replaced with another pumping segment. In some instances, characteristics (e.g., diameter, material, etc.) of the new pumping segment may be different than the pumping segment that is replaced. To accommodate the characteristics of the pumping segment, the gap between the platen (e.g., frame 610) or pressure sensors and the pumping fingers may be required to be adjusted. Accordingly, in convention pumping systems, the hardware/software of the pumping system may be required to be upgraded to accommodate the new characteristics of the new pumping segment.
However, in various embodiments, the thickness of frame 610 is adjustable. That is, frame 610 of one thickness can be swapped out with a frame of a different thickness to accommodate the characteristics of the new pumping segment. In one embodiment, the new frame has a different thickness (than the original frame) to accommodate for the change in the gap between the platen (e.g., frame 610) or pressure sensors and the pumping fingers. Therefore, the hardware/software of the pumping system is not required to be updated in response to replacing pumping segment 130 with another pumping segment with different characteristics.
At 710 of method 700, a non-pinching valve is actuated to a closed position by rotating a slidable cover axially over a housing of said non-pinching valve, wherein the non-pinching valve controls flow of a fluid without requiring pinching of a tube attached to the non-pinching valve. For example, non-pinching valve 340 is initially actuated manually to a closed position such fluid does flow through system 100. In particular, slidable cover 330 is manually axially rotated over housing 310 of non-pinching valve 340. Accordingly, non-pinching valve 340 is able to control flow through system 100 without requiring to pinch a tube (e.g., tube 120) that is attached to the valve.
At 720, the non-pinching valve is placed in a housing of an infusion pump. For example, non-pinching valve 240A is placed in housing 115 of an infusion pump.
At 730, a door of the infusion pump to close access in the housing. For example, door 119 is placed over housing 115 to restrict access housing 115.
At 740, in response to the closing of the door, the non-pinching valve is actuated to an open position, by the door, such that fluid flows through the non-pinching valve. For example, handle 230 is actuated by a feature of door 119 such that fluid flow 125 flows through non-pinching valve 240A.
In one embodiment, at 750, the non-pinching valve is fluidly connected to an IV. For example, non-pinching valve 440B is fluidly connected to an IV such that a fluid in the IV bag is able to be pumped to a patient.
In one embodiment, at 760, the non-pinching valve is fluidly connected to a patient. For example, non-pinching valve 440B is fluidly connected to a patient (not shown) such that a fluid in the IV bag is able to be pumped to a patient via system 100.
Various embodiments of the present invention are thus described. It should be appreciated that embodiments, as described herein, can be utilized or implemented alone or in combination with one another. While the present invention has been described in particular embodiments, it should be appreciated that the present invention should not be construed as limited by such embodiments, but rather construed according to the following claims.
Claims
1. A valve comprising:
- a cylindrical housing comprising a first port and a second port, a first opening of the first port and a second opening of the second port disposed on a same external circular surface of said housing, and first and second fluid channels disposed along a center axis of the housing, wherein the entirety of the housing is cylindrical; and
- a slidable cylindrical cover configured for controlling a flow of a fluid through the first opening of said first port and the second opening of said second port, wherein said slidable cover is slidably disposed on the external circular surface of said housing, and adjacent to and covering the first opening of said first port and the second opening of said second port, wherein said slidable cover comprises: a fluid flow channel comprising a first opening and a second opening, the fluid flow channel configured to receive said fluid flow from the first opening of said first port and transmit said fluid flow to the second opening of said second port when the first opening and the second opening of said fluid flow channel respectively align with the first opening of the first port and the second opening of the second port on the external circular surface of the housing so that the first opening of said fluid flow channel is disposed over the first opening of said first port and the second opening of said fluid flow channel is disposed over the second opening of said second port.
2. The valve of claim 1, wherein said slidable cover is configured to rotate axially with respect to said housing.
3. The valve of claim 1, wherein said slidable cover is configured to rotate axially with respect to said flow of said fluid.
4. The valve of claim 1, wherein said slidable cover comprises:
- a handle protruding from said slidable cover.
5. The valve of claim 1, wherein said fluid flows on an outer surface of said housing when said fluid flow channel is disposed over said first port and said second port.
6. The valve of claim 1, further comprising:
- a connection interface for connecting said valve to a tube.
7. The valve of claim 1, further comprising:
- a graduation marking configured to assist in controlling flow rate of said fluid.
8. The valve of claim 1, further comprising:
- a locking mechanism configured to lock said slidable cover.
9. The valve of claim 1, wherein said slidable cover is further configured to mechanically engage with a door of an infusion pump.
10. The valve of claim 1, wherein said slidable cover is further configured to not allow said fluid to flow through said first port and said second port when said fluid flow channel is not disposed over said first port and said second port.
11. A non-pinching valve system comprising:
- a pump configured for pumping a fluid in a medical environment;
- a tube configured for conveyance of said fluid; and
- a non-pinching valve configured to be disposed in a pump housing and to control a flow of said fluid without requiring pinching of said tube, wherein said tube is releasably attached to said non-pinching valve, said non-pinching valve comprising: a cylindrical housing comprising a first port and a second port, a first opening of the first port and a second opening of the second port disposed on a same external circular surface of said housing, and first and second fluid channels disposed along a center axis of the housing, wherein the entirety of the housing is cylindrical; and a slidable cylindrical cover configured for controlling said flow of said fluid through the first opening of said first port and the second opening of said second port, wherein said slidable cover is slidably disposed on the external circular surface of said housing adjacent to and covering the first opening of said first port and the second opening of said second port, said slidable cover comprising: a fluid flow channel comprising a first opening and a second opening, the fluid flow channel configured to allow said fluid to flow through the first opening of said first port and the second opening of said second port when the first opening and the second opening of said fluid flow channel respectively align with the first opening of the first port and the second opening of the second port on the same external circular surface of the housing so that the first opening of said fluid flow channel is disposed over the first opening of said first port and the second opening of said fluid flow channel is disposed over the second opening of said second port.
12. The non-pinching valve system of claim 11, wherein said non-pinching valve further comprises:
- a handle configured to mechanically engage with a door of said pump.
13. A method of controlling a fluid flow, said method comprising:
- actuating a non-pinching valve to a closed position by rotating a slidable cylindrical cover axially over a cylindrical housing of said non-pinching valve, wherein the entirety of the housing of said non-pinching valve is cylindrical, and wherein said non-pinching valve controls said flow of a fluid without requiring pinching of a tube attached to said non-pinching valve;
- placing said non-pinching valve in a housing of an infusion pump;
- closing a door of said infusion pump to close access in said housing of said infusion pump; and
- in response to said closing of said door, actuating said non-pinching valve to an open position, by said door, such that said fluid flows through said non-pinching valve, wherein actuating said non-pinching valve to the open position comprises sliding the cover on the housing of said non-pinching valve so that a first opening and a second opening of a channel in the cover respectively align with a first opening of a first port and a second opening of a second port disposed on a same external circular surface of the housing of said non-pinching valve, wherein the first opening of the channel in the cover is disposed adjacent to and covering the first opening of the first port and the second opening of the channel in the cover is disposed adjacent to and covering the second opening of the second port on said same external circular surface of said housing of said non-pinching valve, and wherein first and second fluid channels are disposed along a center axis of the housing of said non-pinching valve.
14. The method of claim 13, further comprising:
- fluidly connecting said non-pinching valve to an IV.
15. The method of claim 13, further comprising:
- fluidly connecting said non-pinching valve to a patient.
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Type: Grant
Filed: Jun 15, 2012
Date of Patent: Jul 16, 2019
Patent Publication Number: 20130338624
Assignee: CAREFUSION 303, INC. (San Diego, CA)
Inventors: George Mansour (Pomona, CA), Chris Zollinger (Chino Hills, CA), Jonathan Yeh (Diamond Bar, CA), Christopher J. Clarke (Walton on Thames)
Primary Examiner: Shefali D Patel
Application Number: 13/525,205
International Classification: A61M 39/22 (20060101); A61M 5/142 (20060101); A61M 5/168 (20060101);